Main Street Compounding Pharmacy Recalls Medroxyprogesterone Due to Adverse Reactions
Main Street Compounding Pharmacy is recalling 1,131 units of Medroxyprogesterone 150mg 1ml vials after receiving seven reports of skin abscesses.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The agency classification is FDA Class II, and the source text reports specific adverse reactions (skin abscesses), which aligns with the rubric criteria for Severe severity involving reported injuries.
Plain-English summary
Main Street Family Pharmacy, LLC is recalling 1,131 units of Medroxyprogesterone 150mg 1ml vials. The product was distributed nationwide to specific states including AK, AL, AZ, CA, CO, CT, DC, FL, GA, HI, IL, IN, KS, KY, LA, MA, MD, MN, MO, MS, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, and WV. The recall covers all codes distributed prior to and including 05/23/2013.
The recall was initiated after the firm received seven reports of adverse reactions in the form of skin abscesses. The source text notes these reactions were potentially linked to compounded preservative-free methylprednisolone 80mg/ml 10 ml vials.
Consumers who have this product should contact Main Street Compounding Pharmacy at 888-658-6200 for further instructions.
The recalled product
- Product
- Medroxyprogesterone 150mg 1ml, Main Street Compounding Pharmacy, 126 East Main Street, Newbern, TN 38059, 888-658-6200
- Manufacturer
- Main Street Family Pharmacy, LLC
- Category
- Drug — Compounded Injectable
- Affected units
- 1,131
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- all codes distributed prior to and including 05/23/2013
Distribution
Part of a larger recall action
This product is one of 299 recalled by Main Street Family Pharmacy, LLC under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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